End-stage Renal Disease Clinical Trial
— END-IDLEOfficial title:
End-Stage Renal Disease Intra-dialysis Lifestyle Education Study
Verified date | July 2017 |
Source | Vanderbilt University Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to compare the effects of intra-dialysis yoga to an educational program among patients with end-stage renal disease. The investigators hypothesize that yoga as compared to the educational program will significantly improve quality of life.
Status | Completed |
Enrollment | 67 |
Est. completion date | May 2017 |
Est. primary completion date | May 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Maintenance hemodialysis for =3 or months - Adequately dialyzed (Kt/V =1.2 measured within last 3 months) - Expected to remain in present hemodialysis shift for next 4 months - Expected to remain on hemodialysis for at least 6 months - 18 years or older Exclusion Criteria: - Acute or chronic medical conditions that would make intra-dialysis yoga potentially hazardous - Unstable cardiac disease e.g. angina, life threatening arrhythmia - Chronic lung disease that prevents gentle exercise or deep breathing exercises - Active cerebrovascular disease - Major depression - Chronic symptoms of nausea, vomiting, or diarrhea - Current participation in exercise or mind body program/practice - Cognitive impairment (MME = 24) measured at baseline testing visit |
Country | Name | City | State |
---|---|---|---|
United States | Vanderbilt University Medical Center | Nashville | Tennessee |
Lead Sponsor | Collaborator |
---|---|
Vanderbilt University Medical Center | National Center for Complementary and Integrative Health (NCCIH) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline in Physical Component Summary of Kidney Disease Quality of Life-36 questionnaire at 6 weeks, 12 weeks, and 24 weeks. | The Kidney Disease Quality of Life-36 instrument is a 36-item instrument that contains a generic core (Short Form-12) plus the burden of kidney disease, symptoms/problem of kidney disease, and effects of kidney disease scales. | Baseline, 6 weeks, 12 weeks, and 24 weeks | |
Secondary | Functional Assessment of Chronic Illness Therapy-Fatigue | Questionnaire to assess fatigue among chronic disease patients | Baseline, 6, 12, and 24 weeks | |
Secondary | Profile of Mood States | Questionnaire to assess emotional states | Baseline, 6, 12, and 24 weeks | |
Secondary | Center for Epidemiological Studies Depression | Questionnaire to assess depressive symptoms | Baseline, 6, 12, and 24 weeks | |
Secondary | End-stage renal disease: Patient satisfaction | Questionnaire to assess patient satisfaction with dialysis treatment | Baseline, 6, 12, and 24 weeks | |
Secondary | Pittsburgh Sleep Quality Index | Questionnaire to assess sleep quality | Baseline, 6, 12, and 24 weeks | |
Secondary | Self-efficacy for self-management | Questionnaire to assess self-efficacy for self-management | Baseline, 6, 12, and 24 weeks | |
Secondary | 6-minute walk test | Assessment of physical performance | Baseline, 12, and 24 weeks | |
Secondary | Blood pressure | Baseline and weekly over 12 week study period | ||
Secondary | Measure of endothelial function with flow-mediated vasodilatation | Sub-set of patients will have this assessment of endothelial function which measures percentage change in diameter measured in millimeters | Baseline and 12-weeks | |
Secondary | Measure of arterial stiffness from radial artery based pulse wave analysis | Sub-set of patient will have this assessment of arterial stiffness as augmentation index | Baseline and 12-weeks | |
Secondary | Autonomic tone | Assessment of cardiovagal and sympathoneural functioning including baroreflex and heart rate variability | Baseline and 12-weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04087213 -
Study of HemoCareā¢ Hemodialysis System for Home Nocturnal Dialysis in Patients With ESRD
|
N/A | |
Completed |
NCT02207088 -
Ombitasvir/ABT-450/Ritonavir and Dasabuvir With or Without Ribavirin in HCV Genotype 1-Infected Adults With Chronic Kidney Disease
|
Phase 3 | |
Not yet recruiting |
NCT03090828 -
Economic Evaluation of an Education Platform for Patients With End-stage Renal Disease
|
N/A | |
Completed |
NCT02237521 -
The Effect of the Incretin Hormones on the Endocrine Pancreatic Function During Hyperglycemia in End-stage Renal Disease
|
N/A | |
Withdrawn |
NCT01691196 -
Inflammation in Peritoneal Dialysis Patients: Effect of Obesity
|
||
Completed |
NCT01394341 -
Liraglutide Treatment to Patients With Severe Renal Insufficiency
|
Phase 4 | |
Active, not recruiting |
NCT00247507 -
The Effects of Acetylcysteine on Alleviating Damage of Oxidative Stress in Hemodialysis Patients
|
Phase 4 | |
Completed |
NCT00307463 -
Effects of Strict Volume Control in Hypertensive Hemodialysis Patients on Cardiac Structure and Chronic Inflammation
|
Phase 4 | |
Recruiting |
NCT00155363 -
Effect of Different Hemodialysis Modality on Adiponectin,Vascular Function and Clinical Prognosis
|
Phase 4 | |
Completed |
NCT00234156 -
The Effect of Fructose on Blood Fats in Dialysis Patients and Healthy Volunteers
|
N/A | |
Completed |
NCT00586131 -
Arterial pH and Total Body Nitrogen Balances in APD
|
Phase 4 | |
Active, not recruiting |
NCT05027074 -
Global Study of MK-2060 (Anti-Factor XI Monoclonal Antibody) in Participants With End Stage Renal Disease Receiving Hemodialysis (FXI Hemodialysis Study) (MK-2060-007)
|
Phase 2 | |
Recruiting |
NCT04575077 -
The Role of Hepcidin as a Biomarker to Predict Successful Renal Transplantation
|
||
Enrolling by invitation |
NCT05001009 -
Goals of Care Conversations Study
|
N/A | |
Completed |
NCT01756508 -
Eculizumab for Prevention and Treatment of Kidney Graft Reperfusion Injury
|
Phase 2 | |
Recruiting |
NCT03862859 -
The Danish Warfarin-Dialysis Study - Safety and Efficacy of Warfarin in Patients With Atrial Fibrillation on Dialysis
|
Phase 4 | |
Terminated |
NCT03661229 -
Cardiovascular and Respiratory Assessment Using Biometric Signals in a Non-contact Monitoring Device
|
N/A | |
Completed |
NCT03288922 -
Protein-bound Toxin Removal Between Limited Blood Flow Super High-flux Online HDF and High-Efficiency Online HDF
|
N/A | |
Completed |
NCT02572882 -
Gut Microbiome and p-Inulin in Hemodialysis
|
N/A | |
Completed |
NCT02360748 -
A Plant Based High Protein Diet to Improve Nutritional Outcomes in Peritoneal Dialysis Patients
|
N/A |